2,2,2-Trifluoro-1-(4-fluoro-2-methyl-phenyl)ethanone, with the CAS number 886370-02-1, is an organic compound characterized by its unique fluorinated structure. This compound features a ketone functional group, which contributes to its reactivity and potential applications in organic synthesis. The presence of multiple fluorine atoms enhances its lipophilicity and may influence its biological activity, making it of interest in medicinal chemistry. The compound is likely to exhibit stability under standard conditions, but its reactivity can be influenced by the electron-withdrawing nature of the fluorine substituents. Additionally, the aromatic ring containing a methyl group and a fluorine atom suggests potential for interactions in various chemical environments. As a fluorinated compound, it may also exhibit unique properties such as increased volatility and altered solubility compared to non-fluorinated analogs. Overall, 2,2,2-trifluoro-1-(4-fluoro-2-methyl-phenyl)ethanone represents a class of compounds that are valuable in research and industrial applications, particularly in the development of pharmaceuticals and agrochemicals.

2,2,2-trifluoro-1-(4-fluoro-2-methyl-phenyl)ethanone

886370-02-1: 2,2,2-Trifluoro-1-(4-fluoro-2-methyl-phenyl)ethanone, with the CAS number 886370-02-1, is an organic compound characterized by its unique fluorinated structure. This compound features a ketone functional group, which contributes to its reactivity and potential applications in organic synthesis. The presence of multiple fluorine atoms enhances its lipophilicity and may influence its biological activity, making it of interest in medicinal chemistry. The compound is likely to exhibit stability under standard conditions, but its reactivity can be influenced by the electron-withdrawing nature of the fluorine substituents. Additionally, the aromatic ring containing a methyl group and a fluorine atom suggests potential for interactions in various chemical environments. As a fluorinated compound, it may also exhibit unique properties such as increased volatility and altered solubility compared to non-fluorinated analogs. Overall, 2,2,2-trifluoro-1-(4-fluoro-2-methyl-phenyl)ethanone represents a class of compounds that are valuable in research and industrial applications, particularly in the development of pharmaceuticals and agrochemicals.

CAS 886370-02-1

2,2,2-trifluoro-1-(4-fluoro-2-methyl-phenyl)ethanone

2,2,2-Trifluoro-1-(4-fluoro-2-methylphenyl)ethanone

Ref: IN-DA0049X5